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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1947 1
1949 1
1950 4
1952 1
1956 1
1957 1
1958 1
1960 2
1967 1
1968 1
1969 1
1971 1
1972 1
1975 3
1976 2
1977 3
1978 4
1979 4
1980 3
1981 1
1982 2
1983 5
1984 3
1985 2
1986 3
1987 3
1988 2
1989 6
1990 7
1991 5
1992 6
1993 7
1994 5
1995 5
1996 9
1997 6
1998 13
1999 10
2000 7
2001 9
2002 6
2003 11
2004 15
2005 12
2006 18
2007 13
2008 15
2009 11
2010 10
2011 11
2012 17
2013 20
2014 19
2015 16
2016 13
2017 13
2018 18
2019 18
2020 18
2021 15
2022 11
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Article attribute
Article type
Publication date

Search Results

407 results
Results by year
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Page 1
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M. Campuzano V, et al. Among authors: de michele g. Science. 1996 Mar 8;271(5254):1423-7. doi: 10.1126/science.271.5254.1423. Science. 1996. PMID: 8596916
Spinocerebellar ataxia type 48: last but not least.
De Michele G, Galatolo D, Barghigiani M, Dello Iacovo D, Trovato R, Tessa A, Salvatore E, Filla A, De Michele G, Santorelli FM. De Michele G, et al. Neurol Sci. 2020 Sep;41(9):2423-2432. doi: 10.1007/s10072-020-04408-3. Epub 2020 Apr 27. Neurol Sci. 2020. PMID: 32342324 Review.
Degenerative and acquired sporadic adult onset ataxia.
Lieto M, Roca A, Santorelli FM, Fico T, De Michele G, Bellofatto M, Saccà F, De Michele G, Filla A. Lieto M, et al. Among authors: de michele g. Neurol Sci. 2019 Jul;40(7):1335-1342. doi: 10.1007/s10072-019-03856-w. Epub 2019 Mar 29. Neurol Sci. 2019. PMID: 30927137 Review.
Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review.
Vecchia SD, Tessa A, Dosi C, Baldacci J, Pasquariello R, Antenora A, Astrea G, Bassi MT, Battini R, Casali C, Cioffi E, Conti G, De Michele G, Ferrari AR, Filla A, Fiorillo C, Fusco C, Gallone S, Germiniasi C, Guerrini R, Haggiag S, Lopergolo D, Martinuzzi A, Melani F, Mignarri A, Panzeri E, Pini A, Pinto AM, Pochiero F, Primiano G, Procopio E, Renieri A, Romaniello R, Sancricca C, Servidei S, Spagnoli C, Ticci C, Rubegni A, Santorelli FM. Vecchia SD, et al. Among authors: de michele g. J Neurol. 2022 Jan;269(1):437-450. doi: 10.1007/s00415-021-10792-3. Epub 2021 Sep 6. J Neurol. 2022. PMID: 34487232
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Galatolo D, De Michele G, Silvestri G, Leuzzi V, Casali C, Musumeci O, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Caputi C, Cioffi E, De Michele G, Dotti MT, Fico T, Fiorillo C, Galosi S, Lieto M, Malandrini A, Melone MAB, Mignarri A, Natale G, Pegoraro E, Petrucci A, Ricca I, Riso V, Rossi S, Rubegni A, Scarlatti A, Tinelli F, Trovato R, Tedeschi G, Tessa A, Filla A, Santorelli FM. Galatolo D, et al. Among authors: de michele g. Int J Mol Sci. 2021 Aug 6;22(16):8490. doi: 10.3390/ijms22168490. Int J Mol Sci. 2021. PMID: 34445196 Free PMC article.
Antiphospholipid-related chorea.
Peluso S, Antenora A, De Rosa A, Roca A, Maddaluno G, Brescia Morra V, De Michele G. Peluso S, et al. Among authors: de michele g. Front Neurol. 2012 Oct 22;3:150. doi: 10.3389/fneur.2012.00150. eCollection 2012. Front Neurol. 2012. PMID: 23097646 Free PMC article.
Of cognition and cerebellum in SCA48.
De Michele G, Salvatore E, Cocozza S, Filla A, Santorelli FM. De Michele G, et al. Neurogenetics. 2020 Apr;21(2):145-146. doi: 10.1007/s10048-020-00603-8. Epub 2020 Feb 3. Neurogenetics. 2020. PMID: 32009217 No abstract available.
Spinocerebellar ataxia type 48: last but not least.
De Michele G, Santorelli F. De Michele G, et al. Neurol Sci. 2021 Apr;42(4):1577. doi: 10.1007/s10072-020-04812-9. Epub 2020 Oct 13. Neurol Sci. 2021. PMID: 33048271 No abstract available.
STUB1-Related Ataxias: A Challenging Diagnosis.
Cocozza S, Santorelli FM, De Michele G. Cocozza S, et al. Among authors: de michele g. Mov Disord Clin Pract. 2020 Jul 19;7(6):733-734. doi: 10.1002/mdc3.12992. eCollection 2020 Aug. Mov Disord Clin Pract. 2020. PMID: 32775533 Free PMC article. No abstract available.
407 results